1. Volume 23, Issue 8, Pages 2443-2454 (May 2018)
Nup133 Is Required for Proper Nuclear Pore Basket Assembly and Dynamics in Embryonic Stem Cells 
Benoit Souquet, Ellen Freed, Alessandro Berto, Vedrana Andric, Nicolas Audugé, Bernardo Reina-San-Martin, Elizabeth Lacy, Valérie Doye 
Cell Reports 
Volume 23, Issue 8, Pages (May 2018)
DOI: /j.celrep
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2. Cell Reports 2018 23, 2443-2454DOI: (10.1016/j.celrep.2018.04.070)
Copyright © 2018 The Authors Terms and Conditions

3. Figure 1 NPC Assembly Appears Unaltered in Nup133-Deficient mESCs
(A) Left: representative spinning-disk images (one z section) of co-cultured WT (1A4) and Nup133−/− (#319) mESCs stained for DAPI, Nup133 and Nup96 (top) or Nup98 (bottom); scale bar, 10 μm. Right: signal intensities for Nup96, Nup98, and Nup153 at the NE in WT (1A4) and Nup133−/− (#319) mESCs were quantified for n cells from two or more independent experiments and normalized to the average for WT nuclei in the same field.
(B) Top: representative 3D-SIM images of WT mESCs stained for Nup98, Cyclin B1, and DAPI; scale bar, 10 μm. Bottom left: enlarged views of the NE surface of a G1 cell show Nup98-labeled NPCs and the corresponding spots defined as individual NPCs by Imaris. Bottom right: Imaris-based quantification of the total number of Nup98-labeled NPCs in WT (1A4, JA1) and Nup133−/− (#319, #532) mESCs in G1 and G2 (Experimental Procedures).
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4. Figure 2
3D-SIM Images Reveal a Widespread Overlap in the Patterns of Fluorescence for Nup98 and Nup153 in WT and Nup133−/− mESCs but a Lack of Tpr in About One-Half of the NPCs in Nup133-Deficient mESCs
(A) Representative SIM images of WT (1A4) and Nup133−/− (#319) mESCs double labeled with anti-Nup98 (green) and anti-Nup153 (red) antibodies. The square insets depict the region shown at higher magnification in the three panels to the right; the individual and merged images for Nup98 and Nup153. Scale bar, 10 μm.
(B) Relative numbers of Nup98- and Nup153-labeled NPCs in WT (1A4) and Nup133−/− (#319) mESCs. Numbers of Nup98- and Nup153-labeled NPCs were independently quantitated for 11 WT (1A4) and 12 Nup133−/− (#319) mESCs and the ratio of Nup153 to Nup98-containing NPCs determined for each cell. The average ± SD is presented.
(C) Representative SIM microscopy images of the NE surface of WT (1A4) and Nup133−/− (#319) mESCs stained for Nup98 and Tpr. Scale bar, 2 μm.
(D) Quantification of the total number of Tpr-labeled NPCs in WT and Nup133−/− mESCs during G1 and G2. See also Figure S1A.
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5. Figure 3
The 2-Fold Decrease in Tpr Fluorescence Intensity at the NE in Nup133-Deficient Compared to WT mESCs Is Not Caused by Its Altered Dynamics at NPCs
(A) Representative spinning-disk images (one z section) of WT (1A4) and Nup133−/− (#319) mESCs grown together and stained for Nup133, Nup153, Tpr, and DAPI. Scale bar, 10 μm. Arrowheads point to intranuclear foci labeled by Tpr but not Nup153.
(B) Normalized Tpr signal intensity at the NE in WT (1A4 or HM1) and Nup133−/− (#319 or #14) mESCs. n: number of cells quantified from two or more independent experiments;
(C) Quantification of the fraction of cells containing Tpr-positive and Nup153-negative intranuclear foci in WT and Nup133−/− mESCs. Average ± SD based on analysis of n cells from two or more independent experiments.
(D) Tpr-GFP mislocalization in Nup133−/− mESCs was quantified based on the NE/nucleoplasm intensity ratios acquired on individual live cells (n =) expressing Tpr-GFP.
(E) Top: pseudocolored images of selected time frames (average projection of three z sections used for quantitation) from representative iFRAP experiments performed on WT (HM1) or Nup133−/− (#14) mESCs expressing Tpr-GFP and treated with 50 μM cycloheximide. Time 0 was defined as the first time point after bleach. Scale bar, 10 μm. Bottom: plots of fluorescence decay kinetics from the unbleached region in WT (blue curves) and Nup133−/− (red curves) mESCs. Average normalized fluorescence signals ± SDs were quantified at each acquisition time point as detailed in Experimental Procedures. See also Figure S1.
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6. Figure 4
Nup133 Deficiency Increases Nup153 Dynamics In Vivo in mESCs but Does Not Alter Interactions between Nup153-NTD and the Y-Complex or Tpr In Vitro
(A) Schematic of Nup153 functional domains (BD, binding domain; Mb, membrane). Amino acid numbers refer to human Nup153. See text for details.
(B and C) Top: pseudocolored images of selected time frames from representative iFRAP experiments performed on WT (HM1) or Nup133−/− (#14) mESCs expressing GFP-Nup153 (B) or GFP-Nup153-NTD (C). Time 0 was defined as the first time point after bleach. Scale bar, 10 μm. Middle: plots of fluorescence decay kinetics from the unbleached region in WT (blue curves) and Nup133−/− (red curves) mESCs. Average normalized fluorescence signals ± SDs were quantified at each acquisition time point as detailed in Experimental Procedures. Cells were quantified from three (B) or two (C) independent experiments. Bottom: the fractions of the various GFP-Nup153 or GFP-Nup153-NTD populations exhibiting distinct dynamics at the NE and the half time of residency for the dynamic population (t1/2) were determined based on the fit of the normalized fluorescence signals from the indicated number of WT or Nup133−/− mESCs (Experimental Procedures).
(D) Pull-down experiments using as bait Nup153-NTD (aa 1–245) or (aa 1–339) and whole-cell extracts from WT (HM1) or Nup133−/− (KO, #14) mESCs. Inputs (1× equivalent) and eluates (64× equivalent or 48× equivalent arising from a distinct experiment) were analyzed by western blot using the indicated Y-complex antibodies and Tpr. Anti-Nup98 and GAPDH were used as negative controls (original data are available as Mendeley dataset under
(E) Volcano plot of quantitative mass spectrometry analysis of pull-down experiments using Nup153-NTD (aa 1–339) as bait and whole-cell extracts from WT compared to Nup133−/− mESCs. The curves correspond to the 5% threshold cutoff. Note that, except Nup133, Y-complex Nups (highlighted in purple) and Tpr (highlighted in green) are not significantly different between WT and Nup133−/−-purified fractions. See also Figure S2.
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7. Figure 5 The Mid Domain of Nup133 Is Required for NPC Basket Assembly
(A) Schematic representation of the GFP or mCherry-Nup133 constructs used in this study.
(B) Representative spinning-disk images of HM1 WT mESCs (blue dots) mixed and co-cultured with either Nup133−/− mESCs (#14; red dots, left panels) or with Nup133−/− mESCs stably expressing mCherry-Nup133 (mCh-Nup133 FL-a; green dots, middle panels) or mCherry-Nup133ΔMid (mCh-Nup133ΔMid-a; orange dots, right panels) and immunostained for Nup133 and Tpr. One z section of acquisition is shown. Scale bar, 10 μm.
(C) Normalized Tpr signal intensity at the NE in WT (1A4) and Nup133−/− (#319) mESCs, either control (Ø) or stably expressing GFP-Nup133 (FL), GFP-Nup133ΔN or ΔMid or ΔC. The numbers of cells quantified (n), of independent experiments (exp), and, when relevant, of independent clones analyzed (nb#) are indicated.
(D) Tpr and Nup133 normalized intensities at the NE in the indicated cell lines were quantified and plotted as in (C).
(E) Plots of GFP-Nup153 fluorescence decay kinetics from the unbleached region in Nup133−/− mESCs (#14) stably expressing either mCherry-Nup133 (FL-a and FL-b, left) or mCherry-Nup133ΔMid (ΔMid-a and ΔMid-b, right) at comparable level (Figure S3C). Average normalized fluorescence signals ± SDs are plotted at each time point and were quantified from the indicated number of cells (n =). Average values from iFRAP experiments on WT (HM1, blue dots) and Nup133−/− mESCs (#14, red dots) arising from Figure 4B are plotted on both graphs as references. See also Figure S3.
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